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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 881593Generated: November 2, 2026

Acetic Anhydride → HCID 58437297, compound

https://huagongshe.com/reaction/881593

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium HydroxideHCID 14798—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantHCID 58437409HCID 58437409—
SolventPyridineHCID 1049—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58437297HCID 5843729765.8%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 3-formyl-1H-indole-5-carboxylic acid benzyl ester (4.3 g) and pyridine (4.8 g) in tetrahydrofuran (60 ml) was added hydroxylamine hydrochloride (1.6 g) at room temperature and this mixture was stirred at 80° C. overnight. Acetic anhydride was added to reaction mixture at the same temperature and this mixture was stirred for 8 hours. After cooling to ambient temperature, 1 mol/L sodium hydroxide solution (20 mL) was added to this mixture and resulting mixture was extracted with diethyl ether. The organic layer was washed with brine, and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure and this residue was purified by column chromatography on silica gel (eluent: n-hexane/ethyl acetate) to give the title compound (2.8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993616B2
Source datasetuspto-grants-2015_03
ORD IDord-4dc95cd17c0547da82a180164fb1d772
Source noteuspto-grants-2015_03